There are several methods available for the prediction of whether an amino acid substitution is pathogenic or benign. These methods are mostly based on phylogenetic information (Multiple sequence alignments), and some methods combine structural information and/or functional annotation with the sequence analysis in order to reach more accurate results.
nsSNPAnalyzer |
http://snpanalyzer.utmem.edu/ |
(Bao, et al., 2005) |
Panther |
http://www.pantherdb.org/tools/csnpScoreForm.jsp |
(Thomas, et al., 2003) |
PhD-SNP |
http://gpcr.biocomp.unibo.it/cgi/predictors/PhD-SNP/PhD-SNP.cgi |
(Capriotti, et al., 2006) |
PMut |
http://mmb2.pcb.ub.es:8080/PMut/ |
(Ferrer-Costa, et al., 2005) |
PolyPhen |
http://coot.embl.de/PolyPhen/ |
(Ramensky, et al., 2002) |
SIFT |
http://blocks.fhcrc.org/sift/SIFT.html |
(Ng and Henikoff, 2001) |
SNPs3D |
http://www.snps3d.org/ |
(Yue, et al., 2006) |
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